cortisol Assay kit(Chemiluminescence Immunoassay Method） (UDI 06978465236026)
Manufactured by Shenzhen Dake Medical Technology Co.,Ltd
Device Regulatory Overview
The cortisol Assay kit(Chemiluminescence Immunoassay Method） (Model/Catalog Number: 2×50 test) is a medical device manufactured by Shenzhen Dake Medical Technology Co.,Ltd. This product is indexed under FDA Product Code / Category Classification W0102060203 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2×50 test
- Product Code / EMDN
- W0102060203
- Device Name
- cortisol Assay kit(Chemiluminescence Immunoassay Method）
- Database Sync Date
- 2026-08-09 18:01:07
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of cortisol Assay kit(Chemiluminescence Immunoassay Method）?
The registered manufacturer of record for cortisol Assay kit(Chemiluminescence Immunoassay Method） is Shenzhen Dake Medical Technology Co.,Ltd.
What is the Primary UDI-DI identifier for cortisol Assay kit(Chemiluminescence Immunoassay Method）?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06978465236026.
What classification code is assigned to this device?
This device is registered under product classification code W0102060203.
Similar Classification Devices (W0102060203)
Other Devices by Shenzhen Dake Medical Technology Co.,Ltd
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